BACTERIAL BREAKDOWN OF BENOMYL .1. PURE CULTURES

被引:22
作者
FUCHS, A
DEVRIES, FW
机构
[1] Laboratory of Phytopathology, Agricultural University, Wageningen
来源
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY | 1978年 / 44卷 / 3-4期
关键词
D O I
10.1007/BF00394306
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
With different soil and water samples as inoculum and the benzimidazole fungicides benomyl (either as Benlate or as the pure compound) and thiabendazole as selective agents, a large number of, mainly fluorescent, Pseudomonas strains were isolated which nearly all were able to grow in a mineral medium with benomyl as the sole source of carbon. However, no growth occurred with any of a series of other benzimidazole compounds, viz. benzimidazole, 2-aminobenzimidazole (2-AB), thiabendazole and fuberidazole. Although benomyl-or rather its non-enzymatic breakdown product methyl benzimidazol-2-yl carbamate (MBC)-was partially degraded to 2-AB, most probably n-butylamine, which arises after splitting off of the butylcarbamoyl side chain, was the actual carbon source for the Pseudomonas isolates. When incorporated in a lactate medium, 2-AB markedly inhibited the growth of Pseudomonas spp. at a concentration of 250 μg/ml, with complete inhibition being attained at 500 μg/ml. For Bacillus spp. grown in liquid peptone media benzimidazole compounds were inhibitory at concentrations of 500-1000 μg/ml, with a toxicity increasing in the order: benzimidazole <thiabendazole <MBC <2-AB. © 1978 H. Veenman & Zonen B.V. Publishers.
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页码:283 / 292
页数:10
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